128581-33-9

Basic information

• Product Name: 1H-Indole, 1-(3,4-dimethoxybenzoyl)-2,3-dihydro-
• CAS NO: 128581-33-9
• Molecular Formula: C17H17NO3
• Molecular Weight: 283.327
• Mol File: 128581-33-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 1-(3,4-dimethoxybenzoyl)-2,3-dihydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 1-(3,4-dimethoxybenzoyl)-2,3-dihydro-(128581-33-9)
• EPA Substance Registry System: 1H-Indole, 1-(3,4-dimethoxybenzoyl)-2,3-dihydro-(128581-33-9)

Safety Data

• Hazardous Substances Data: 128581-33-9(Hazardous Substances Data)

Usage

Chemical family

Indole

Common uses

Organic synthesis, pharmaceutical research

Known for

Potential bioactive properties

Studied for

Potential use in pharmaceutical development

Unique

Structure and properties valuable for further research and application in medicine and drug development.

Upstream product

• 869468-93-9 trifluoro-methanesulfonic acid 2-(2-methoxycarbonyloxy-ethyl)-phenyl ester 
• 1521-41-1 veratramide 
• 869469-11-4 trifluoro-methanesulfonic acid 2-(2-oxo-ethyl)-phenyl ester 
• 869469-13-6 trifluoro-methanesulfonic acid 2-(2-hydroxy-ethyl)-phenyl ester 
• 109586-43-8 o-(2-propenyl)phenyl trifluoromethanesulfonate 
• 1745-81-9 o-Allylphenol 
• 3535-37-3 3,4-dimethoxybenzoic acid chloride 
• 496-15-1 1-indoline 
• 93-07-2 Veratric acid 

Downstream Products

• 101442-38-0 (3,4-dimethoxyphenyl)(1H-indol-1-yl)methanone 
• 80787-57-1 pratorinine 

Relevant articles and documents

Electrochemical Total Synthesis of Pyrrolophenanthridone Alkaloids: Controlling the Anodically Initiated Electron Transfer Process

Electrochemical intramolecular C(sp2)-H cross-coupling and dehydrogenative indole synthesis were developed. Both reactions were initiated by anodic oxidation of the same electron-rich indoline moiety, but the product selectivity was controlled

A domino amidation route to indolines and indoles: Rapid syntheses of anhydrolycorinone, hippadine, oxoassoanine, and pratosine

(Chemical Equation Presented) When subjected to palladium-catalyzed amidation conditions, 2-triflyloxy phenethyl carbonates undergo, in addition to the expected aryl cross-coupling, an additional amidation with net displacement of the carbonate. The result is a one-step synthesis of indolines which may be oxidized to indoles. The utility of the procedure is illustrated by the two- or three-step syntheses of anhydrolycorinone, hippadine, oxoassoanine, and pratosine.